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      <title>Rett Syndrome by CEANNA TOBIN</title>
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      <description></description>
      <language>en-us</language>
      <pubDate>2019-02-19 18:54:39 UTC</pubDate>
      <lastBuildDate>2024-05-23 16:36:49 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Definition </title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/332871602</link>
         <description><![CDATA[<div>Rett Syndrome is a Nero-developmental condition that primarily affects girls </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-02-19 18:58:18 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/332871602</guid>
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      <item>
         <title>What is the genetic cause</title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/332875660</link>
         <description><![CDATA[<div>Caused by mutations in the MecP2 Gene. the gene has the instructions to a protein (MecP2) needed for development of the  nervous system and normal brain function </div>]]></description>
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         <pubDate>2019-02-19 19:04:21 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/332875660</guid>
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         <title>Symptoms </title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/333749651</link>
         <description><![CDATA[<div>Rapid regression in language and fine motor skills, repetitive hand movements,fits of screaming and crying,episodic seizure, and inability to walk </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-02-21 17:26:19 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/333749651</guid>
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         <title>Diagnosis</title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/333760773</link>
         <description><![CDATA[<div>Affected girls have a normal development during the first 6 to 18 months of life </div>]]></description>
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         <pubDate>2019-02-21 17:43:25 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/333760773</guid>
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         <title>Treatment  </title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/333765281</link>
         <description><![CDATA[<div>project Orphan Anesthesia </div>]]></description>
         <enclosure url="" />
         <pubDate>2019-02-21 17:51:02 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/333765281</guid>
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         <title>Cure </title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/333768001</link>
         <description><![CDATA[<div>Scientists are still trying to find to a cure</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-02-21 17:55:44 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/333768001</guid>
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      <item>
         <title>Impact</title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/333769631</link>
         <description><![CDATA[<div>it will make the person need more help, and the person won't live alone</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-02-21 17:58:29 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/333769631</guid>
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      <item>
         <title>Interesting fact </title>
         <author>3340351</author>
         <link>https://padlet.com/3340351/cppxy55kq2mt/wish/333771849</link>
         <description><![CDATA[<div> Only 1% of cases are inherited from the parents</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-02-21 18:02:18 UTC</pubDate>
         <guid>https://padlet.com/3340351/cppxy55kq2mt/wish/333771849</guid>
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